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Acta Pharmaceutica Sinica ; (12): 484-489, 2008.
Article in Chinese | WPRIM | ID: wpr-277826

ABSTRACT

In present study, we investigated the mechanism of regulating HIF-1alpha expression by hydroxysafflor yellow A (HSYA) in Eahy 926 cell line under 1% O2 hypoxia. Eahy 926 cells were incubated with HSYA (100, 10 and 1 micromol x L(-1)) under hypoxia for the indicated time after treatment. Cell proliferation rate was detected using MTT assays. VHL and p53 location and protein expression were analyzed by immunocytochemical stain. HIF-1alpha, VHL and p53 mRNA expression were detected by RT-PCR. Protein expression of HIF-1alpha, VHL and p53 were assayed by Western blotting method. HSYA at 100 micromol x L(-1) increased Eahy 926 cells proliferation rate under hypoxia. HIF-1alpha mRNA and protein expression were up-regulated in the presence of HSYA. VHL, p53 mRNA and protein expression decreased significantly after 8 hours of treatment under hypoxia. HSYA protected Eahy 926 cells from hypoxia, and up-regulated HIF-1alpha expression partially via its inhibition of VHL and p53 expression.


Subject(s)
Humans , Carthamus tinctorius , Chemistry , Cell Hypoxia , Cell Line , Cell Proliferation , Chalcone , Pharmacology , Endothelial Cells , Cell Biology , Metabolism , Flowers , Chemistry , Hypoxia-Inducible Factor 1, alpha Subunit , Genetics , Plants, Medicinal , Chemistry , Quinones , Pharmacology , RNA, Messenger , Metabolism , Tumor Suppressor Protein p53 , Genetics , Umbilical Veins , Cell Biology , Up-Regulation , Von Hippel-Lindau Tumor Suppressor Protein , Genetics
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